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1.1 KiB
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1 line
1.1 KiB
JSON
{"Adverse Reaction Reports": 114, "Company": "MODERNA", "Deaths": 0, "Disabilities": 0, "Hospitalizations": 1, "Life-Threatening Illnesses": 0, "batchcode": "AU5552B", "histogram": {"Bradycardia": 1, "COVID-19": 1, "Dizziness": 1, "Expired product administered": 1, "Exposure to SARS-CoV-2": 1, "Extra dose administered": 3, "Fall": 1, "Feeling hot": 1, "Generalised tonic-clonic seizure": 1, "Hypoxia": 1, "Inappropriate schedule of product administration": 1, "Incorrect dose administered": 89, "Insurance issue": 1, "Manufacturing issue": 6, "Nausea": 2, "No adverse event": 22, "Oxygen saturation decreased": 1, "Product administered to patient of inappropriate age": 1, "Product dispensing error": 8, "Product dose omission issue": 1, "Product label issue": 2, "Product storage error": 1, "Productive cough": 1, "Pyrexia": 1, "Rales": 1, "Rash": 2, "Rash papular": 1, "Rash pruritic": 1, "SARS-CoV-2 test positive": 1, "Seizure": 1, "Serum sickness": 1, "Skin discolouration": 1, "Syncope": 1, "Underdose": 5, "Unevaluable event": 1, "Urticaria": 1, "Vomiting": 2, "Wrong product administered": 2}} |